The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

2701–2725 of 36527

  • SevereFDA (Devices)·Z-1456-2025·2025-04-16

    Medline medical procedure kits with Medtronic Aortic Root Cannula recalled

    Medline Industries is recalling medical procedure kits containing a Medtronic Aortic Root Cannula due to a Class I defect. The kits were distributed to healthcare facilities in nine states.

    Product
    Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Drugs)·D-0355-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled for Sterility Assurance Defect

    Somerset Therapeutics is recalling 997 vials of Haloperidol Decanoate Injection 50mg/mL nationwide due to lack of assurance of sterility following bacterial contamination detected in a media fill validation test.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0360-2025·2025-04-16

    Proactiv Skin Smoothing Exfoliator recalled for benzene contamination

    Alchemee, LLC is recalling Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) due to the presence of benzene, a known chemical contaminant.

    Product
    Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g), UPC 8 42944 10223 1; Distributed by Alchemee, LLC, Santa Monica, CA 90401,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0354-2025·2025-04-16

    Methocarbamol Injection USP Recalled Due to Sterility Assurance Concerns

    Somerset Therapeutics is recalling Methocarbamol Injection USP (1,000 mg/10 mL vials) nationwide due to lack of assurance of sterility following bacterial contamination in media fill testing.

    Product
    METHOCARBAMOL — METHOCARBAMOL (METHOCARBAMOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1512-2025·2025-04-16

    Hippo 072 Aspiration System recalled for distal tip detachment risk

    Qapel Medical Inc. is recalling the Hippo 072 Aspiration System and related components because the aspiration catheter distal tip may detach, potentially causing vessel rupture or vasospasm.

    Product
    Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including Cheetah Delivery Tool, REF: AP6072-132. 072 Aspiration Tubing, REF: APT-95
    Category
    Medical Device
    Distribution
    29 states
  • SevereFDA (Drugs)·D-0358-2025·2025-04-16

    Haloperidol Decanoate Injection Recalled Due to Sterility Concerns

    Somerset Therapeutics is recalling Haloperidol Decanoate Injection (100 mg/mL, 1 mL vials) due to lack of assurance of sterility caused by bacterial contamination detected in media fill testing.

    Product
    HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E027000·2025-04-14

    Nova Bus Recalls ZF Brake Chambers Due to Air Leak Risk

    Nova Bus is recalling specific ZF brake chambers sold as replacement parts for buses because improper manufacturing may cause air leaks, increasing the risk of unexpected braking, overheating, or fire.

    Product
    SERVICE BRAKES, AIR:DISC:CHAMBER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V236000·2025-04-11

    Ford Recalls 2017-2018 F-150, Expedition, Navigator for Brake Leak

    Ford is recalling 2017-2018 F-150, Expedition, and Lincoln Navigator vehicles because a brake master cylinder defect may cause fluid leaks, reducing braking ability and increasing crash risk.

    Product
    FORD — FORD, LINCOLN EXPEDITION, F-150, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V241000·2025-04-11

    Jayco Recalls 2025-2026 Entegra Motorhomes Due to Fuel Leak Risk

    Jayco is recalling 2025-2026 Entegra Aspire, Anthem, and Cornerstone motorhomes because a fuel filter housing may leak, increasing fire risk.

    Product
    ENTEGRA — ENTEGRA ANTHEM, CORNERSTONE, redundant ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V240000·2025-04-11

    Mercedes-Benz Recalls 2024 E-Class Models for Electrical Fire Risk

    Mercedes-Benz is recalling 2024 E 350 and E 450 vehicles because improperly secured electrical ground connections may overheat and increase the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V238000·2025-04-11

    Ford Recalls 2024-2025 E-Transit Chassis Due to Battery Fire Risk

    Ford is recalling 2024-2025 E-Transit Chassis vehicles because battery tray rails may crack, allowing water entry that could cause a fire.

    Product
    FORD — FORD E-TRANSIT CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V235000·2025-04-10

    Hyundai IONIQ 5 N may brake weakly and keep accelerating

    Hyundai is recalling certain 2025 IONIQ 5 N vehicles because software may reduce braking performance with left-foot braking active and the vehicle may continue to accelerate.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V232000·2025-04-10

    Cadillac LYRIQ stabilizer bar bracket bolts may loosen and separate

    GM is recalling certain 2023-2025 Cadillac LYRIQ vehicles because front stabilizer bar bracket bolts may loosen and separate from the vehicle frame.

    Product
    CADILLAC — CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V234000·2025-04-10

    Acura ZDX stabilizer bar bracket bolts may loosen and separate

    Honda is recalling certain 2024 Acura ZDX vehicles because passenger-side front stabilizer bar bracket bolts may loosen and separate from the vehicle frame.

    Product
    ACURA — ACURA ZDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V216000·2025-04-09

    McLaren brake lines may be routed to the wrong side

    McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.

    Product
    MCLAREN — MCLAREN ARTURA, 720S SPIDER, GT, 600LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0675-2025·2025-04-09

    Choshiya Shiba Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Shiba Zuke Prepared Mix Vegetables (1,000 cases) because they are missing the required "Keep Refrigerated" statement on the label. Non-shelf stable vegetables could be improperly stored without this critical labeling information.

    Product
    Choshiya branded "SHIBA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535128
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0678-2025·2025-04-09

    Packaged Vegetables Recalled for Missing Refrigeration Label Statement

    AKT Trading Inc. is recalling Choshiya branded Soft Tsubozuke Prepared Mix Vegetables due to missing "Keep Refrigerated" statement on labels. Non-shelf stable vegetables lacking this statement may spoil or develop harmful bacteria if stored improperly.

    Product
    Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0688-2025·2025-04-09

    Tostitos Cantina Chips Recalled for Undeclared Milk Allergen

    Frito-Lay is recalling 1,295 bags of Tostitos Cantina Traditional Yellow Corn Tortilla Chips because milk was not declared on the label. Affected products were distributed across 13 states.

    Product
    Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz. (368.5) UPC 0 28400-52848 1. Frito-Lay, Inc., Plano, TX 75024-4099.
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0680-2025·2025-04-09

    Choshiya Prepared Bamboo Shoots Recalled Due to Missing Keep Refrigerated Label

    Choshiya branded menma (prepared bamboo shoots) are being recalled because the label fails to include the required 'Keep Refrigerated' statement. Improper storage of this non-shelf-stable product could lead to foodborne illness.

    Product
    Choshiya branded "MENMA AJITSUKE PREPARED BAMBOO SHOOTS" UPC# JANCODE 4983673527325
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0676-2025·2025-04-09

    Choshiya Aokappa Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Aokappa Zuke Prepared Mix Vegetables because the product label lacks a 'Keep Refrigerated' statement, risking improper storage of non-shelf-stable vegetables.

    Product
    Choshiya branded "AOKAPPA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535135
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1499-2025·2025-04-09

    Anesthesia Circuit Kit Flex EPA recalled due to breathing hose cracking

    Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intend
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0679-2025·2025-04-09

    Choshiya Rakkyo Zuke Prepared Vegetables Recalled for Missing Refrigeration Label

    Choshiya brand rakkyo zuke prepared vegetables are being recalled due to missing 'Keep Refrigerated' label statements. These non-shelf-stable vegetables may spoil if not properly refrigerated.

    Product
    Choshiya branded "RAKKYO ZUKE PREPARED VEGETABLES" UPC# JANCODE 4983673526021
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1497-2025·2025-04-09

    Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide